Related by context. All words. (Click for frequent words.) 69 de novo mutations 69 chromosome aberrations 68 somatic mutations 67 gene rearrangements 66 spontaneous mutations 66 DNA rearrangements 66 chromosomal rearrangements 65 genetic rearrangements 65 primate genomes 65 mutations 65 VHL gene 64 genomic variants 64 molecular abnormalities 64 non coding RNA 64 genetic recombination 64 noncoding RNAs 64 genomic deletions 64 chromosomal translocations 64 genomic alterations 63 mtDNA mutations 63 ependymomas 63 epigenetic modification 63 microcephalin 63 Alu elements 63 chromosomal rearrangement 63 miRNA expression 63 missense mutations 63 microRNAs miRNAs 63 beta1 integrin 63 histone modifications 63 aneuploid cells 63 hamartomas 63 neural crest 63 monogenic 63 epigenetic changes 63 virulence genes 62 gene duplications 62 KRAS oncogene 62 epigenetic alterations 62 genetic alterations 62 chromatin structure 62 chromosomal aberrations 62 MLL gene 62 previously uncharacterized 62 medulloblastomas 62 3'UTR 62 germline mutations 62 segmental duplications 62 inherited mutations 62 epigenetic regulation 62 mosaicism 62 chromosomal anomalies 62 somatic mutation 62 epigenetic modifications 62 luminal cells 62 microRNA expression 62 genomic instability 62 pathogenic mutations 62 epigenetic markers 62 gene expression patterns 62 genetic loci 62 genotoxic stress 61 p# mutations 61 LIS1 61 aneuploidies 61 miRNA genes 61 epigenetic mechanisms 61 tRNA synthetases 61 yeast genome 61 epigenetic marks 61 mammalian genomes 61 fungal genomes 61 chromosome rearrangements 61 metazoan 61 molecular subtypes 61 seminomas 61 TP# mutation 61 neurofibroma 61 DNA methylation patterns 61 microarray experiments 61 chromosome translocations 61 ALK gene 61 methylation patterns 61 BRCA1 BRCA2 61 HAR1 61 promoter hypermethylation 61 indels 61 vertebrate embryos 61 splice junctions 60 ALK mutations 60 organism genome 60 bacterial genomes 60 RNA splicing 60 skin fibroblasts 60 MC4R gene 60 mRNA molecules 60 phenotypic expression 60 microdeletions 60 spontaneous mutation 60 genetic aberrations 60 sequence homology 60 MAPCs 60 microRNA molecules 60 metazoans 60 mutational 60 mitochondrial gene 60 hypermethylation 60 hypermethylated 60 epigenetically 60 paralogs 60 melanocytic 60 PML RARA 60 quasispecies 60 genome rearrangements 60 KCNH2 60 LRRK2 gene 60 eukaryotic cells 60 karyotypes 60 MSH2 60 intracellular bacteria 60 phylogenetic analyzes 60 chromosomal deletions 60 mammary cells 60 antigenic shift 60 insertions deletions 60 precursor lesions 59 Velculescu 59 multicellular organisms 59 atypical hyperplasia 59 differential gene expression 59 basal cells 59 chromosomal instability 59 genetic mutations 59 underlying molecular mechanisms 59 CHD7 59 Hox gene 59 RNA sequences 59 untranslated regions 59 causative mutations 59 viral genomes 59 genetic manipulations 59 clefting 59 neoplastic 59 chromosome abnormalities 59 endogenous retroviruses 59 microdeletion 59 mammary cancers 59 teratoma 59 mutated genes 59 coevolution 59 conserved sequences 59 cisplatin resistant 59 osteosarcomas 59 chromosome #q#.# [001] 59 gastric carcinomas 59 primary cilia 59 TCF#L# gene 59 neurofibromas 59 MLL2 59 mitochondrial mutations 59 epigenetic silencing 59 #q#.# [002] 59 malignant phenotype 59 MAPK pathway 59 deleterious mutations 59 splice variants 59 monogenic disorders 59 PrPSc 59 recombination hotspots 59 FGFs 58 yeast prions 58 X inactivation 58 BARD1 58 CYP#D# gene 58 NSCLC tumors 58 synaptogenesis 58 embryonal 58 neural cells 58 ABCB1 gene 58 genetic locus 58 mutant huntingtin protein 58 RNA viruses 58 posttranslational modifications 58 molecular pathways 58 heterochromatin 58 Drosophila genome 58 cDNAs 58 mitochondrial DNA mtDNA 58 polyploid 58 maternally inherited 58 FGFR2 gene 58 micro RNAs 58 protein conformation 58 evolutionary lineages 58 synovial cells 58 mRNA decay 58 nucleotide substitutions 58 tau aggregates 58 protein coding RNAs 58 proto oncogene 58 Cathepsin B 58 transgenic mouse models 58 MECP2 gene 58 intergenic 58 epithelial tumors 58 gene fusions 58 #q#.# [001] 58 malaria parasite genome 58 biochemical assays 58 Transcriptome 58 short hairpin RNAs 58 RNA polymerases 58 mutation 58 ribosomal DNA 58 non coding RNAs 58 rearrangements 58 genetic alteration 58 morphologically 58 receptor ligand 58 SLITRK1 58 genetic determinants 58 Clusterin 58 PTEN gene 58 cell nuclei 58 bone marrow mesenchymal stem 58 alternative splicing 58 micro RNA 58 hyperplastic 58 antibody mediated 58 malignant transformation 58 underlying pathophysiology 58 nanobacteria 58 transposable elements 58 dendritic spine 58 epigenome 58 M. pneumoniae 58 endocasts 58 paraganglioma 58 MLH1 58 cell signaling pathways 58 epigenetic inheritance 58 ncRNAs 58 genomic variation 58 genetic polymorphisms 58 chromosomal abnormalities 58 mitochondrial dysfunction 58 translocations 58 melanocyte 58 PALB2 58 genetic underpinnings 58 hamartoma 58 pre malignant lesions 58 structural rearrangements 58 brain lesions 58 gene amplification 57 eukaryote 57 phylogenetic trees 57 normal prion protein 57 PTPN# 57 APOL1 57 biologic pathways 57 BDNF gene 57 coding sequences 57 acinar 57 molecular mechanisms underlying 57 Genetic mutations 57 ribosomal RNA rRNA 57 NF1 gene 57 evolvability 57 epistasis 57 endometrial cancers 57 coding exons 57 leiomyomas 57 Wnts 57 #S rRNA 57 modifier genes 57 Fragile X gene 57 DEAR1 57 amyloid fibrils 57 Jhdm2a 57 granule cells 57 eukaryotic organisms 57 prion infection 57 V#F mutation 57 Cryptococcus neoformans 57 #S rRNA gene 57 malignant prostate 57 quantitative trait loci 57 ARID1A 57 DSBs 57 MeCP2 gene 57 K ras mutations 57 piRNAs 57 FGFR2 57 gene expression profiles 57 neuronal dysfunction 57 ovarian pancreatic 57 chromosomal regions 57 biochemical mechanisms 57 druggable targets 57 granulosa cell 57 BRAF V#E 57 pathogenic mechanisms 57 antisense RNA 57 aneuploid 57 mitochondrial metabolism 57 mutagenesis 57 sea urchin genome 57 HDAC enzyme 57 alpha synuclein gene 57 proteomes 57 PIK3CA 57 precancerous stem cells 57 mammary stem cells 57 ribosomal RNA 57 microglial cells 57 S. sanguinis 57 hammerhead ribozyme 57 FMR1 gene 57 subcellular compartments 57 positional cloning 57 TTR gene 57 p#/CBP 57 TFIIH 57 aneuploidy 57 trophoblasts 57 biochemical abnormalities 57 deacetylation 57 filamentous fungi 57 multigene 57 misfolding 57 heterochromatic 57 transcriptional regulation 57 chromosome #p#.# 57 myopathies 57 glycan 57 signaling cascades 57 H#K#me# 57 meningiomas 57 viral proteins 57 C. neoformans 57 Induced pluripotent stem cells 57 causative genes 57 cAMP signaling 57 ERK2 57 monozygotic twins 57 cathepsins 57 JAK STAT 57 muscular dystrophies 57 multiprotein complex 57 organogenesis 57 potent inhibitors 57 allelic variants 57 Colon polyps 57 HGPS 57 mesenchymal cell 57 platypus genome 57 retroviral vectors 56 herpesviruses 56 mucinous 56 epigenomes 56 neuropathologic 56 malaria parasite Plasmodium falciparum 56 neural crest cells 56 oligodendrogliomas 56 tumor suppressor protein 56 molecular biomarkers 56 branching morphogenesis 56 cellular pathways 56 gene mutations 56 Arabidopsis genome 56 PTEN protein 56 shRNAs 56 premalignant 56 lincRNAs 56 neural crest stem cells 56 SLC#A# gene [001] 56 gliosis 56 phenotypic differences 56 DNA demethylation 56 leiomyoma 56 GPC5 56 CALHM1 56 OGG1 56 mRNA transcripts 56 noncoding RNA 56 amino acid substitutions 56 siRNA knockdown 56 TMPRSS2 ERG 56 HOTAIR 56 RNA transcripts 56 commensal bacteria 56 EGF receptors 56 noncoding 56 multiplex ligation dependent 56 motor neuron degeneration 56 tyrosine phosphorylation 56 neuroblastoma tumors 56 MDR1 56 chromosomal mutations 56 protein misfolding 56 genomic loci 56 eccrine 56 prion strains 56 tumor suppressor genes 56 carcinoids 56 TP# gene 56 HLA genes 56 familial clustering 56 STK# [002] 56 miRNAs 56 Skeletal muscle 56 BRAF gene 56 phenotypic variation 56 nucleosome positioning 56 malignant lesions 56 apoptotic pathway 56 biopsied tissue 56 UVB induced 56 podocytes 56 breast cancer genes BRCA1 56 phylogenies 56 Chromosomal 56 neutralizing antibody responses 56 CPEB 56 IDH1 gene 56 kinase gene 56 mitochondrial proteins 56 operons 56 mammary duct 56 embryonic germ 56 gastrulation 56 mitochondrial disorders 56 MC1R gene 56 uPAR 56 telomere dysfunction 56 epigenomic 56 enterotypes 56 Prox1 56 SATB1 56 GNAQ 56 susceptibility genes 56 Single Nucleotide Polymorphisms SNPs 56 conformational changes 56 genetic polymorphism 56 genomewide association studies 56 neurite outgrowth 56 intronic 56 amyloid deposition 56 X chromosome inactivation 56 JAK mutations 56 MYCN amplification 56 CRISPR 56 JAK2 enzyme 56 progranulin gene 56 Wnt signaling pathway 56 ADPKD 56 RNA transcription 56 Genetic variations 56 Pten 56 FGFR3 56 histone acetylation 56 morphologies 56 FUS1 56 misregulation 56 genital tract infections 56 Histologically 56 biologic pathway 56 mitogen activated protein kinases 56 genes BRCA1 56 Xenopus laevis 56 genetic makeups 56 Kufs disease 56 x ray crystallographic 56 subventricular zone 56 CNVs 56 von Hippel Lindau 56 egg follicles 56 neuroblastomas 56 BRCA1 mutations 56 NR#A# gene 56 incidentalomas 56 beta amyloid peptides 56 microsatellite instability 56 mesotheliomas 56 Prion diseases 56 amyloid deposits 56 genomic imprinting 56 CGG repeats 56 X4 viruses 56 NFTs 56 diploid cells 56 Hox genes 56 Htt 56 histone modification 56 functional polymorphism 56 MT1 MMP 56 dedifferentiation 56 genomewide 56 epithelial tissues 56 choroid plexus 56 histone H4 56 Mitochondrial 56 homologies 56 5 methylcytosine 56 molecular underpinnings 56 exons 56 CpG island 56 intercellular signaling 56 osteoblastic 56 zebrafish larvae 56 breast cancer subtypes 56 MiRNAs 55 polyploidy 55 PARP inhibition 55 multi celled organisms 55 DARPP 55 neural progenitor cells 55 RNA ribonucleic acid 55 transcriptomes 55 synaptic proteins 55 carcinoid 55 Brain metastases 55 cardiac fibroblasts 55 vitamin D receptors 55 Helicobacter 55 genomically 55 glucose abnormalities 55 pRb 55 genetic abnormalities 55 histocompatibility 55 S. maltophilia 55 lymphoid cells 55 nucleotide sequence 55 neuronal stem cells 55 #p#.# [002] 55 neuropsychiatric diseases 55 nucleoli 55 overactivation 55 LRRK2 mutation 55 roundworm C. elegans 55 tumor subtypes 55 LRP5 55 indel 55 phosphatases 55 aberrant methylation 55 hypomethylation 55 protein tyrosine phosphatases 55 generalized vitiligo 55 prokaryotic 55 hypocretin neurons 55 morphologic 55 NFKBIA 55 schwannomas 55 substrate specificity 55 miRNA molecules 55 holoprosencephaly 55 microglial 55 coding genes 55 ADAMTS# 55 clinicopathologic 55 hippocampal formation 55 white matter hyperintensities 55 chromosome condensation 55 IDH1 mutation 55 tau protein tangles 55 sRNA 55 cnidarians 55 genes encode proteins 55 palladin 55 WDR# 55 segmental duplication 55 gastric carcinoma 55 osteochondromas 55 N. gonorrhoeae 55 cis regulatory 55 fibroma 55 RUNX3 55 mechanotransduction 55 tissue biopsies 55 Shiekhattar 55 neuronal plasticity 55 primordial germ cells 55 amyloid cascade 55 neurexins 55 pancreatic endocrine 55 blastomeres 55 Sanger sequencing 55 ataxias 55 pituitary adenomas 55 germline cells 55 neural progenitors 55 SCN5A 55 mutant enzymes 55 hair follicle stem cells 55 Polycomb proteins 55 pulmonary metastases 55 prion gene 55 EZH2 55 morphological traits 55 allele frequencies 55 proliferative disorders 55 phenotypically 55 GBM tumors 55 X ray crystallographic 55 phthalate syndrome 55 UCRs 55 histologic subtypes 55 Epstein Barr Virus EBV 55 HbF 55 myelofibrosis polycythemia vera 55 tumor suppressor gene 55 menin 55 unspecialized cells 55 oncogenic transformation 55 DNA methylation 55 thyroid carcinoma 55 GISTs 55 morphogens 55 hantaviruses 55 nongenetic 55 #S rDNA 55 morphometrics 55 HPRT gene 55 epigenetic reprogramming 55 neural progenitor 55 cytosine methylation 55 BRAF protein 55 KCNQ1 55 Immunohistochemical analysis 55 chimeric mice 55 Genetic variants 55 PCA3 gene 55 TMPRSS2 ERG fusion 55 FTLD 55 mutant proteins 55 enzymatic pathways 55 glial tumors 55 constitutively expressed 55 endospores 55 inactivating mutations 55 inactive X chromosome 55 ribozyme 55 gene deletions 55 renal cell carcinomas 55 budding yeast 55 sporadic ALS 55 cardiac progenitor cells 55 epithelial tissue 55 p tau 55 gamma globin gene 55 RNA molecules 55 mitochondrial fusion 55 Microarray analysis 55 granzyme B 55 Caenorhabditis elegans 55 huntingtin 55 intracellular signaling 55 polyglutamine diseases 55 Confocal microscopy 55 uncharacterized 55 ependymal cells 55 GBA mutations 55 Hurthle cell 55 NF kB signaling 55 histone methylation 55 susceptibility loci 55 TET2 55 Trichomonas 55 neoplastic transformation 55 astrocytic 55 gene locus 55 Fas ligand 55 transgene expression 55 multisensory integration 55 mRNA expression 55 EML4 ALK 55 ERBB2 55 papillomas 55 malignant tissues 55 TMEM#B 55 Mutational 55 neurodevelopmental disorders 55 HER2 gene 55 multinucleated giant cells 55 exfoliative glaucoma 55 lung adenocarcinomas 55 inbred strains 55 pulmonary metastasis 55 haematopoietic 55 meiotic recombination 55 dyskeratosis congenita 55 microchimerism 55 H#Y 55 alpha synuclein protein 55 bioinformatic analysis 55 myofibroblasts 55 CDK4 55 vertebrate genomes 55 MAP kinases 55 polymerases 55 Mycoplasma genitalium 55 BCL#A 55 causal variants 55 ubiquitylation 55 #p#.# [001] 55 PON1 55 transgenic rats 55 p# activation 55 miRs 55 eukaryotic genomes 55 chromatin modifications 55 SVZ 55 prostate cancer CaP 55 lymphocytic 55 array CGH 55 methylated DNA 55 protein isoforms 55 ultraconserved elements 55 androgen receptor AR 55 chromosomal aberration 55 clinicopathological 55 sporadic Creutzfeldt Jakob 55 chromosome #q# [001] 55 transcriptional regulators 55 embryological 55 trypanosome 55 non mammalian vertebrates 54 symbiont 54 Genetic profiling 54 susceptibility locus 54 Hashimoto thyroiditis 54 missense mutation 54 nonviral 54 MeCP2 protein 54 DCIS lesions 54 ductal carcinomas 54 benign polyps 54 neuroimaging studies 54 sphingolipid 54 Kabuki syndrome 54 vascular dysfunction 54 normal karyotype 54 MTHFR 54 oncogenes 54 CSHL scientists 54 allelic variation 54 genetic heterogeneity 54 STAT4 54 CD# expression [001] 54 Argonaute proteins 54 neuroligins 54 VNTR 54 adipokines 54 trophoblast 54 RNA strands 54 morphogen 54 IgA deficiency 54 bilaterians 54 androgen signaling 54 LRP6 54 alternatively spliced 54 rifamycins 54 mycoplasmas 54 CDH1 54 Wnt proteins 54 immunohistochemical analysis 54 pathogenetic mechanisms 54 COL#A# 54 atherosclerotic lesions 54 da mage 54 bdelloid 54 CagA 54 primary cilium 54 electrophysiological recordings 54 dopamine D4 receptor 54 neuroimaging techniques 54 M. genitalium 54 thermodynamic stability 54 gut microbiota 54 autism susceptibility genes 54 epilepsies 54 FGFR1 54 telomere DNA 54 splice variant 54 silico prediction 54 dissociative disorders 54 nucleolar 54 Cytogenetic 54 chimp genomes 54 protein alpha synuclein 54 childhood leukemias 54 apoE 54 ncRNA 54 evolutionarily conserved 54 insertional mutagenesis 54 Aravinda Chakravarti 54 neuronal circuits 54 genes differentially expressed 54 experimentally validated 54 metaplasia 54 cypin 54 diagnostic biomarker 54 TSC1 54 radial glia 54 genomic rearrangement 54 hippocampal cells 54 DLC1 54 multicellular animals 54 proteomic analysis 54 body louse genome 54 Hakonarson 54 microbial genomes 54 teratomas 54 germline mutation 54 Phenotypic 54 mycobacterial 54 RT PCR assay 54 mTOR signaling pathway 54 transfusion syndrome 54 carbohydrate antigens 54 X. laevis 54 nematode worms 54 biological molecules 54 gene expression 54 neuroepithelial cells 54 nonmelanoma skin cancers 54 #q# deletion 54 neoplastic cells 54 L. pneumophila 54 5 hydroxymethylcytosine 54 MMP# 54 bile acid metabolism 54 soluble proteins 54 chitinase 54 carcinoid tumor 54 replicase 54 HipA 54 endostatin 54 genes encoding 54 extramedullary 54 EBNA1 54 intracellular protein 54 familial ALS 54 Methylation 54 CYP#A# gene 54 DNMT1 54 effector molecules 54 electron microscopic 54 HOX genes 54 TXNIP 54 globin genes 54 FXTAS 54 vertebrate evolution 54 Gliomas 54 oscillatory 54 autoinflammatory diseases 54 serine protease 54 myeloproliferative disorders 54 hematopoietic cells 54 phenotypes 54 abnormal proteins 54 fruitfly Drosophila 54 neoplasms 54 parthenogenetic stem cells 54 cDNA microarray 54 c Myb 54 nucleolar dominance 54 Brd4 54 trypanosomes 54 circadian genes 54 micronuclei 54 homodimers 54 neuropilin 54 pleiotropic 54 Western blotting 54 etiologic factors 54 herpes viruses 54 schwannoma 54 karyotype 54 breast carcinomas 54 miRNA expression patterns 54 chimerism 54 chromosomal DNA 54 Cyclin E 54 transgenic mouse model 54 adhesion proteins 54 β1 54 tumor biopsies 54 chromosomal 54 chromosomal alterations 54 cDNA libraries 54 sexually dimorphic 54 Karlseder 54 engineered RAP peptides 54 papillary carcinoma 54 KIAA# 54 autosomal recessive 54 synthetases 54 Cyclin D1 54 bronchial epithelial cells 54 ribonucleic acids 54 morphological 54 embryonic tissues 54 spectroscopic techniques 54 DUX4 54 mutated BRCA1 54 Li Fraumeni syndrome 54 Joubert syndromes 54 COX enzymes 54 K ras gene 54 metabolomic profiles 54 synovial 54 fetal chromosomal 54 H2AX 54 ChIP chip 54 MGUS 54 proteolytic cleavage 54 A. thaliana 54 TOP2A 54 BCL6 gene 54 MTHFR gene 54 synuclein 54 Loeys Dietz syndrome 54 cytologically 54 Cysts 54 causative gene 54 huntingtin gene 54 cellular organelles 54 MEF2A 54 carbonate globules 54 amino acid sequences 54 histone code 54 neuromuscular junction 54 chimeric protein 54 protein biosynthesis 54 protein misfolding diseases 54 endosymbiosis 54 DNA sequences 54 genetic variants 54 situs inversus 54 electrophysiologic 54 centromeres 54 pharmacodynamic biomarkers 54 PTEN tumor suppressor 54 Trichophyton rubrum 54 copper zinc superoxide 54 glioblastoma tumor 54 tumorigenicity 54 SPINK1 54 SCN1A 54 leukaemias 54 Cryptococcus 54 prostate carcinoma 54 Histologic 54 striated muscle 54 hyperactivation 54 TOP2A gene 54 oncoprotein 54 nucleotide sequences 54 Plasmodium parasites 54 macaque genome 54 Foxp3 54 LMNA 54 impair fertility 54 thyroid nodules 54 lung adenocarcinoma 54 prokaryotic organisms 54 IRF6 54 chromosomal imbalance 54 cervical lymph nodes 54 metabolomic 54 protein encoded 54 EBV infection 54 heritable disorders 54 HSF1 54 orthologous 54 Mitochondrial diseases 54 recessive mutation 54 Dysregulation 54 hepatic stellate cells 54 ultrastructure 54 ribosomal subunits 54 Li Fraumeni 54 TACI mutations 54 FGF signaling 54 genomic proteomic 54 cellularity 54 OPHN1 54 neoplastic lesions 54 Mammalian 54 trophoblast cells 54 cellular microenvironment 54 NEIL1 54 exocytosis 54 ADAM# 54 SGK1 54 heritable variation 54 plexiform neurofibromas